Glasgow/DryWeek1
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In the afternoon, all modellers were shown some Wetlab techniques for the sake of a more thorough understanding of the processes involved. | In the afternoon, all modellers were shown some Wetlab techniques for the sake of a more thorough understanding of the processes involved. | ||
| - | Our experiment was to extract plasmids from a number of different bacterial [[Glasgow/ | + | Our experiment was to extract plasmids from a number of different bacterial [[Glasgow/Wetlab/Week1 cultures]]. |
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Revision as of 12:43, 28 September 2007
| https://static.igem.org/mediawiki/2007/thumb/c/cc/Uog.jpg/50px-Uog.jpg | Back To Glasgow's Main Page | Back To Glasgow's Drylab's Log |
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Contents |
Week 1
02/07
After a brief re-introduction to the Laboratory and our project proposal, we outlined a ******6-PHASE********* approach to guide our practice over the summer.
From here the Modellers began working on basic Matlab modelling tutorials, designed by Xu Gu, to allow all modellers to reach a satisfactory ability. By the end of the day we had completed a number of [http://en.wikipedia.org/wiki/Law_of_mass_action Mass-action] programs using the ode45 funtion and grasped the translation from basic notaion into [http://en.wikipedia.org/wiki/Substrate_%28biochemistry%29 Substrate], [http://en.wikipedia.org/wiki/Enzyme Enzyme] and S/E-complex notation.
03/07
We developed our modelling techniques by programming responses to basic [http://en.wikipedia.org/wiki/Metabolic_pathway metabolic] and [http://en.wikipedia.org/wiki/Cell_signaling signalling] pathways. We then learnt more precise techniques of modelling, e.g. accuracy and tolerace variance and noting parameters. We then covered if while and switch functions.
04/07
We were introduced to the [http://en.wikipedia.org/wiki/Nested_function 'Nested Functions'] to allow for simpler programming, and the basic ideas behind Sensitivity of output due to a range of possible values of varying constants.
In the afternoon, all modellers were shown some Wetlab techniques for the sake of a more thorough understanding of the processes involved.
Our experiment was to extract plasmids from a number of different bacterial Glasgow/Wetlab/Week1 cultures.
05/07
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